InChI key
JXMZUNPWVXQADG-UHFFFAOYSA-N
InChI
1S/C6H4INO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H
SMILES string
[O-][N+](=O)c1ccccc1I
assay
97%
form
solid
bp
288-289 °C (lit.)
mp
49-51 °C (lit.)
functional group
iodo, nitro
Quality Level
Application
用 1-碘-2-硝基苯一步合成 2-(2-吡啶基)-3H-吲哚-3-酮 N-氧化物 。1-碘-2-硝基苯在 PEG 3400 (聚乙二醇))–Cs 2 CO 3 – 铜催化剂存在下微波活化合成 1-(2-硝基苯基)-1 H -吲哚 。
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
此项目有
Dardan Hetemi et al.
Acta chimica Slovenica, dec(4), 818-824 (2018-01-11)
An efficient, versatile and non-destructive in situ method in reaction monitoring using vibrational spectroscopy is described. A Suzuki cross-coupling reaction was monitored in which the substrate 1-iodo-2-nitrobenzene reacted with the electrophile phenylboronic acid to form the product 2-nitrobiphenyl. To hasten
A one-step synthesis of 2-(2-Pyridyl)-3H-indol-3-one N-oxide: is it an efficient spin trap for hydroxyl radical?
G M Rosen et al.
The Journal of organic chemistry, 65(14), 4460-4463 (2000-07-13)
PEG3400-Cs2CO3: an efficient and recyclable microwave-enhanced catalytic system for ligand-free Ullmann arylation of indole and benzimidazole.
Colacino E, et al.
Tetrahedron, 66(21), 3730-3735 (2010)
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